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rabbit polyclonal antibodies against fn1  (Proteintech)


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    Structured Review

    Proteintech rabbit polyclonal antibodies against fn1
    Rabbit Polyclonal Antibodies Against Fn1, supplied by Proteintech, used in various techniques. Bioz Stars score: 98/100, based on 456 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibodies against fn1/product/Proteintech
    Average 98 stars, based on 456 article reviews
    rabbit polyclonal antibodies against fn1 - by Bioz Stars, 2026-02
    98/100 stars

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    98
    Proteintech rabbit polyclonal antibodies against fn1
    Rabbit Polyclonal Antibodies Against Fn1, supplied by Proteintech, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Proteintech rabbit polyclonal anti fibronectin 1 fn1
    Increased <t>FN1</t> and LTBP-4 in cerebral arterioles of CRHTRA1 rats. Measurement of FN1 expression in pial arteries was conducted using automated threshold intensity quantification. Vessels were captured from regions of interest identified during vessel thickness quantification. Compared to WT rats (A), CRHTRA1 rats showed significantly increased fluorescent intensity of FN1 in pial arteries (B, C). Similarly, compared to WT rats (D), CRHTRA1 rats showed significantly increased fluorescent intensity of LTBP-4 in pial arteries (E, F). Scale bars = 100 µm. Data shown as mean ± SD of vessels imaged from n = 6 CRHTRA1 rats and n = 6 WT rats. * p < 0.05; *** p < 0.001.
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    Proteintech rabbit polyclonal anti fn1

    Rabbit Polyclonal Anti Fn1, supplied by Proteintech, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Boster Bio rabbit polyclonal anti fibronectin

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    Proteintech fibronectin 1 fn1 rabbit polyclonal antibody

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    Proteintech polyclonal rabbit fn1 antibody
    Activation of lactate signal promotes pulmonary fibrosis in mice. ( A ) Timeline of GPR81 agonist-treated mouse lung fibrosis model. ( B ) Quantification of hydroxyproline content in mouse right inferior lobe ( n = 4 mice per group). ( C ) Quantification of total cells in BALF ( n = 3). ( D ) Protein concentration in BALF ( n = 3). ( E ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( F ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( G and H ) qPCR analysis of α-SMA, Col1a1, and <t>Fn1</t> mRNA expression levels and immunofluorescence staining of lipid droplet in mouse lung tissue samples ( n = 4). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.
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    Cusabio mouse anti fn1
    Activation of lactate signal promotes pulmonary fibrosis in mice. ( A ) Timeline of GPR81 agonist-treated mouse lung fibrosis model. ( B ) Quantification of hydroxyproline content in mouse right inferior lobe ( n = 4 mice per group). ( C ) Quantification of total cells in BALF ( n = 3). ( D ) Protein concentration in BALF ( n = 3). ( E ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( F ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( G and H ) qPCR analysis of α-SMA, Col1a1, and <t>Fn1</t> mRNA expression levels and immunofluorescence staining of lipid droplet in mouse lung tissue samples ( n = 4). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.
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    Thermo Fisher antibody anti-human-fn1 (rabbit polyclonal)

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    fn1  (Cusabio)
    92
    Cusabio fn1
    The compound-target-signaling networks generated using Cytoscape_v3.8.0. The active compounds cyclopamine, quercetin, kaempferol and mairin could target 12 IDD disease genes including HMGB1, PTEN, IGFBP6, FGFR3, COL3A1, MMP2, SMAD2, HSPG2, GPC1, <t>FN1,</t> CUL4B, CSGALNACT1 (Among 13 target genes, INTS8 did not have pathway enrichment). The compound-targeted disease genes were enriched in 23 pathways.
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    Image Search Results


    Increased FN1 and LTBP-4 in cerebral arterioles of CRHTRA1 rats. Measurement of FN1 expression in pial arteries was conducted using automated threshold intensity quantification. Vessels were captured from regions of interest identified during vessel thickness quantification. Compared to WT rats (A), CRHTRA1 rats showed significantly increased fluorescent intensity of FN1 in pial arteries (B, C). Similarly, compared to WT rats (D), CRHTRA1 rats showed significantly increased fluorescent intensity of LTBP-4 in pial arteries (E, F). Scale bars = 100 µm. Data shown as mean ± SD of vessels imaged from n = 6 CRHTRA1 rats and n = 6 WT rats. * p < 0.05; *** p < 0.001.

    Journal: Cerebral Circulation - Cognition and Behavior

    Article Title: A novel gene edited rat model of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)

    doi: 10.1016/j.cccb.2025.100401

    Figure Lengend Snippet: Increased FN1 and LTBP-4 in cerebral arterioles of CRHTRA1 rats. Measurement of FN1 expression in pial arteries was conducted using automated threshold intensity quantification. Vessels were captured from regions of interest identified during vessel thickness quantification. Compared to WT rats (A), CRHTRA1 rats showed significantly increased fluorescent intensity of FN1 in pial arteries (B, C). Similarly, compared to WT rats (D), CRHTRA1 rats showed significantly increased fluorescent intensity of LTBP-4 in pial arteries (E, F). Scale bars = 100 µm. Data shown as mean ± SD of vessels imaged from n = 6 CRHTRA1 rats and n = 6 WT rats. * p < 0.05; *** p < 0.001.

    Article Snippet: Extracellular matrix (ECM) protein expression was examined using either rabbit polyclonal anti-fibronectin-1 (FN1) (ProteinTech, 15613–1-AP, 1:200) or mouse monoclonal anti-LTBP-4 (R&D Systems, Minneapolis, MN, AF2885, 1:100).

    Techniques: Expressing

    Journal: iScience

    Article Title: Mechanism of hsa_circ_0069443 promoting early pregnancy loss through ALKBH5/FN1 axis in trophoblast cells

    doi: 10.1016/j.isci.2024.111608

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-FN1 , Proteintech , Cat#:15613-1-AP; RRID: AB_2105691.

    Techniques: Recombinant, Magnetic Beads, cDNA Synthesis, SYBR Green Assay, Membrane, Blocking Assay, Red Blood Cell Lysis, Selection, Methylation, Extraction, Cell Counting, CCK-8 Assay, Software

    Activation of lactate signal promotes pulmonary fibrosis in mice. ( A ) Timeline of GPR81 agonist-treated mouse lung fibrosis model. ( B ) Quantification of hydroxyproline content in mouse right inferior lobe ( n = 4 mice per group). ( C ) Quantification of total cells in BALF ( n = 3). ( D ) Protein concentration in BALF ( n = 3). ( E ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( F ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( G and H ) qPCR analysis of α-SMA, Col1a1, and Fn1 mRNA expression levels and immunofluorescence staining of lipid droplet in mouse lung tissue samples ( n = 4). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.

    Journal: Journal of Molecular Cell Biology

    Article Title: CCT6A alleviates pulmonary fibrosis by inhibiting HIF-1α-mediated lactate production

    doi: 10.1093/jmcb/mjae021

    Figure Lengend Snippet: Activation of lactate signal promotes pulmonary fibrosis in mice. ( A ) Timeline of GPR81 agonist-treated mouse lung fibrosis model. ( B ) Quantification of hydroxyproline content in mouse right inferior lobe ( n = 4 mice per group). ( C ) Quantification of total cells in BALF ( n = 3). ( D ) Protein concentration in BALF ( n = 3). ( E ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( F ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( G and H ) qPCR analysis of α-SMA, Col1a1, and Fn1 mRNA expression levels and immunofluorescence staining of lipid droplet in mouse lung tissue samples ( n = 4). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.

    Article Snippet: FN1 , Polyclonal rabbit , Proteintech, 15613-1-AP , 1:2000.

    Techniques: Activation Assay, Protein Concentration, Staining, Western Blot, Marker, Expressing, Immunofluorescence

    Cct6a restores BLM-induced lung fibrosis in mice. ( A ) Timeline of AAV-treated mouse lung fibrosis model. ( B ) Hydroxyproline in the right inferior lobe (Vehicle Sal n = 7, Cct6a Sal n = 8, Vehicle BLM n = 8, Cct6a BLM n = 7). ( C ) Total cell counts in BALF ( n = 7 mice per group). ( D ) Protein concentration in BALF (Vehicle Sal n = 7, Cct6a Sal n = 7, Vehicle BLM n = 8, Cct6a BLM n = 9). ( E ) Representative images of micro CT scans of mouse lung density ( n = 3). ( F ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Boxed regions in the right superior panel are panoramic images of the lung tissue sections. Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( G ) Lactate level in mouse serum (Vehicle Sal n = 8, Cct6a Sal n = 10, Vehicle BLM n = 9, Cct6a BLM n = 10). ( H ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( I ) qPCR analysis of Col1a1, Col3a1, Fn1, and Ctgf mRNA expression levels in the lung homogenate ( n = 6). ( J ) Immunoblot analysis of Vhl, Hif-1α, and Ldha protein levels in whole lung lysates ( n = 3). ( K ) Immunofluorescence staining of lipid droplet in mouse lung sections ( n = 3). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.

    Journal: Journal of Molecular Cell Biology

    Article Title: CCT6A alleviates pulmonary fibrosis by inhibiting HIF-1α-mediated lactate production

    doi: 10.1093/jmcb/mjae021

    Figure Lengend Snippet: Cct6a restores BLM-induced lung fibrosis in mice. ( A ) Timeline of AAV-treated mouse lung fibrosis model. ( B ) Hydroxyproline in the right inferior lobe (Vehicle Sal n = 7, Cct6a Sal n = 8, Vehicle BLM n = 8, Cct6a BLM n = 7). ( C ) Total cell counts in BALF ( n = 7 mice per group). ( D ) Protein concentration in BALF (Vehicle Sal n = 7, Cct6a Sal n = 7, Vehicle BLM n = 8, Cct6a BLM n = 9). ( E ) Representative images of micro CT scans of mouse lung density ( n = 3). ( F ) Representative images of H&E and Masson's Trichrome staining in mouse lung sections ( n = 3). Boxed regions in the right superior panel are panoramic images of the lung tissue sections. Scale bar, 50 μm. The Ashcroft score was determined to indicate the severity of fibrosis. ( G ) Lactate level in mouse serum (Vehicle Sal n = 8, Cct6a Sal n = 10, Vehicle BLM n = 9, Cct6a BLM n = 10). ( H ) Western blotting and quantification of fibrosis marker expression in whole lung lysates ( n = 3). ( I ) qPCR analysis of Col1a1, Col3a1, Fn1, and Ctgf mRNA expression levels in the lung homogenate ( n = 6). ( J ) Immunoblot analysis of Vhl, Hif-1α, and Ldha protein levels in whole lung lysates ( n = 3). ( K ) Immunofluorescence staining of lipid droplet in mouse lung sections ( n = 3). Scale bar, 50 μm. * P < 0.05, ** P <0.01, *** P < 0.001, **** P <0.0001.

    Article Snippet: FN1 , Polyclonal rabbit , Proteintech, 15613-1-AP , 1:2000.

    Techniques: Protein Concentration, Micro-CT, Staining, Western Blot, Marker, Expressing, Immunofluorescence

    Primers and oligonucleotides.

    Journal: Journal of Molecular Cell Biology

    Article Title: CCT6A alleviates pulmonary fibrosis by inhibiting HIF-1α-mediated lactate production

    doi: 10.1093/jmcb/mjae021

    Figure Lengend Snippet: Primers and oligonucleotides.

    Article Snippet: FN1 , Polyclonal rabbit , Proteintech, 15613-1-AP , 1:2000.

    Techniques:

    List of antibodies used in this study.

    Journal: Journal of Molecular Cell Biology

    Article Title: CCT6A alleviates pulmonary fibrosis by inhibiting HIF-1α-mediated lactate production

    doi: 10.1093/jmcb/mjae021

    Figure Lengend Snippet: List of antibodies used in this study.

    Article Snippet: FN1 , Polyclonal rabbit , Proteintech, 15613-1-AP , 1:2000.

    Techniques: Ubiquitin Proteomics

    Journal: eLife

    Article Title: CHD-associated enhancers shape human cardiomyocyte lineage commitment

    doi: 10.7554/eLife.86206

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-human-FN1 (Rabbit polyclonal) , Thermo Fisher , Cat#PA5-29578 , WB(1:1000).

    Techniques: Hybridization, Knock-Out, Sequencing, Recombinant, Plasmid Preparation, Software, Electrophoresis, Quantitation Assay, Imaging, Microscopy

    The compound-target-signaling networks generated using Cytoscape_v3.8.0. The active compounds cyclopamine, quercetin, kaempferol and mairin could target 12 IDD disease genes including HMGB1, PTEN, IGFBP6, FGFR3, COL3A1, MMP2, SMAD2, HSPG2, GPC1, FN1, CUL4B, CSGALNACT1 (Among 13 target genes, INTS8 did not have pathway enrichment). The compound-targeted disease genes were enriched in 23 pathways.

    Journal: Journal of Orthopaedic Translation

    Article Title: Pharmacological network analysis of the functions and mechanism of kaempferol from Du Zhong in intervertebral disc degeneration (IDD)

    doi: 10.1016/j.jot.2023.01.002

    Figure Lengend Snippet: The compound-target-signaling networks generated using Cytoscape_v3.8.0. The active compounds cyclopamine, quercetin, kaempferol and mairin could target 12 IDD disease genes including HMGB1, PTEN, IGFBP6, FGFR3, COL3A1, MMP2, SMAD2, HSPG2, GPC1, FN1, CUL4B, CSGALNACT1 (Among 13 target genes, INTS8 did not have pathway enrichment). The compound-targeted disease genes were enriched in 23 pathways.

    Article Snippet: The following primary antibodies were used in this study: p16 (CSB-PA003618, CUSABIO, Wuhan, China), p21 (ab109520, Abcam, Cambridge, UK), Rb (ab224426, Abcam), hTERT (DF7129, Affinity Biotech), Nrf2 (CSB-RA225569A0HU,Cusabio), HO-1 (10701-1-AP, Proteintech), NQO-1 (11451-1-AP, Proteintech), SOD1 (10269-1-AP, Proteintech), SOD2 (ab227091, Abcam), Cleaved-caspase 3 (ab2302, Abcam), Caspase 3 (ab13847, Abcam), Bax (50599-2-Ig, Proteintech), Bcl-2 (12789-1-AP, Proteintech), aggrecan (13880-1-AP, Proteintech), collagen II (CSB-PA005739ESR2HU, Cusabio), SOX9 (ab185966, Abcam), FN1 (AF5335, Affinity Biotech), MMP2 (CSB-PA003258, Cusabio), MMP3 (17873-1-AP, Proteintech), MMP13 (CSB-PA07029A0Rb, Cusabio), ADAMTS-4 (DF6986, Affinity Biotech), ADAMTS-5 (DF13268, Affinity Biotech), p-p38 (AF4001, Affinity Biotech), p38 (14064-1-AP, Proteintech), p-JNK (AF3318, Affinity Biotech), JNK (AF6319, Affinity Biotech), p-ERK1/2 (sc-81492, Santa Cruz, Dallas, DX, USA), ERK1/2 (16443-1-AP, Proteintech).

    Techniques: Generated

    Compound-target-signaling networks.

    Journal: Journal of Orthopaedic Translation

    Article Title: Pharmacological network analysis of the functions and mechanism of kaempferol from Du Zhong in intervertebral disc degeneration (IDD)

    doi: 10.1016/j.jot.2023.01.002

    Figure Lengend Snippet: Compound-target-signaling networks.

    Article Snippet: The following primary antibodies were used in this study: p16 (CSB-PA003618, CUSABIO, Wuhan, China), p21 (ab109520, Abcam, Cambridge, UK), Rb (ab224426, Abcam), hTERT (DF7129, Affinity Biotech), Nrf2 (CSB-RA225569A0HU,Cusabio), HO-1 (10701-1-AP, Proteintech), NQO-1 (11451-1-AP, Proteintech), SOD1 (10269-1-AP, Proteintech), SOD2 (ab227091, Abcam), Cleaved-caspase 3 (ab2302, Abcam), Caspase 3 (ab13847, Abcam), Bax (50599-2-Ig, Proteintech), Bcl-2 (12789-1-AP, Proteintech), aggrecan (13880-1-AP, Proteintech), collagen II (CSB-PA005739ESR2HU, Cusabio), SOX9 (ab185966, Abcam), FN1 (AF5335, Affinity Biotech), MMP2 (CSB-PA003258, Cusabio), MMP3 (17873-1-AP, Proteintech), MMP13 (CSB-PA07029A0Rb, Cusabio), ADAMTS-4 (DF6986, Affinity Biotech), ADAMTS-5 (DF13268, Affinity Biotech), p-p38 (AF4001, Affinity Biotech), p38 (14064-1-AP, Proteintech), p-JNK (AF3318, Affinity Biotech), JNK (AF6319, Affinity Biotech), p-ERK1/2 (sc-81492, Santa Cruz, Dallas, DX, USA), ERK1/2 (16443-1-AP, Proteintech).

    Techniques: Activity Assay, Migration

    Effects of Kaempferol IL-1β-induced ECM deposition NPCs were exposed to IL-1β stimulation (10 ​ng/ml, 24 ​h), treated with 10 ​μM kaempferol, and examined for the mRNA and protein levels of aggrecan, collagen II, SOX9, FN1 (A–B), MMP3, MMP13, ADAMTS-4, and ADAMTS-5 (C–D) using qRT-PCR and Immunoblotting, respectively. . One-way ANOVA followed by Tukey's post hoc test. N ​= ​3, ∗∗p ​< ​0.01, compared to PBS group; #p ​< ​0.05, ##p ​< ​0.01, compared with IL-1β group.

    Journal: Journal of Orthopaedic Translation

    Article Title: Pharmacological network analysis of the functions and mechanism of kaempferol from Du Zhong in intervertebral disc degeneration (IDD)

    doi: 10.1016/j.jot.2023.01.002

    Figure Lengend Snippet: Effects of Kaempferol IL-1β-induced ECM deposition NPCs were exposed to IL-1β stimulation (10 ​ng/ml, 24 ​h), treated with 10 ​μM kaempferol, and examined for the mRNA and protein levels of aggrecan, collagen II, SOX9, FN1 (A–B), MMP3, MMP13, ADAMTS-4, and ADAMTS-5 (C–D) using qRT-PCR and Immunoblotting, respectively. . One-way ANOVA followed by Tukey's post hoc test. N ​= ​3, ∗∗p ​< ​0.01, compared to PBS group; #p ​< ​0.05, ##p ​< ​0.01, compared with IL-1β group.

    Article Snippet: The following primary antibodies were used in this study: p16 (CSB-PA003618, CUSABIO, Wuhan, China), p21 (ab109520, Abcam, Cambridge, UK), Rb (ab224426, Abcam), hTERT (DF7129, Affinity Biotech), Nrf2 (CSB-RA225569A0HU,Cusabio), HO-1 (10701-1-AP, Proteintech), NQO-1 (11451-1-AP, Proteintech), SOD1 (10269-1-AP, Proteintech), SOD2 (ab227091, Abcam), Cleaved-caspase 3 (ab2302, Abcam), Caspase 3 (ab13847, Abcam), Bax (50599-2-Ig, Proteintech), Bcl-2 (12789-1-AP, Proteintech), aggrecan (13880-1-AP, Proteintech), collagen II (CSB-PA005739ESR2HU, Cusabio), SOX9 (ab185966, Abcam), FN1 (AF5335, Affinity Biotech), MMP2 (CSB-PA003258, Cusabio), MMP3 (17873-1-AP, Proteintech), MMP13 (CSB-PA07029A0Rb, Cusabio), ADAMTS-4 (DF6986, Affinity Biotech), ADAMTS-5 (DF13268, Affinity Biotech), p-p38 (AF4001, Affinity Biotech), p38 (14064-1-AP, Proteintech), p-JNK (AF3318, Affinity Biotech), JNK (AF6319, Affinity Biotech), p-ERK1/2 (sc-81492, Santa Cruz, Dallas, DX, USA), ERK1/2 (16443-1-AP, Proteintech).

    Techniques: Quantitative RT-PCR, Western Blot

    Table S1 The primers for qRT-PCR

    Journal: Journal of Orthopaedic Translation

    Article Title: Pharmacological network analysis of the functions and mechanism of kaempferol from Du Zhong in intervertebral disc degeneration (IDD)

    doi: 10.1016/j.jot.2023.01.002

    Figure Lengend Snippet: Table S1 The primers for qRT-PCR

    Article Snippet: The following primary antibodies were used in this study: p16 (CSB-PA003618, CUSABIO, Wuhan, China), p21 (ab109520, Abcam, Cambridge, UK), Rb (ab224426, Abcam), hTERT (DF7129, Affinity Biotech), Nrf2 (CSB-RA225569A0HU,Cusabio), HO-1 (10701-1-AP, Proteintech), NQO-1 (11451-1-AP, Proteintech), SOD1 (10269-1-AP, Proteintech), SOD2 (ab227091, Abcam), Cleaved-caspase 3 (ab2302, Abcam), Caspase 3 (ab13847, Abcam), Bax (50599-2-Ig, Proteintech), Bcl-2 (12789-1-AP, Proteintech), aggrecan (13880-1-AP, Proteintech), collagen II (CSB-PA005739ESR2HU, Cusabio), SOX9 (ab185966, Abcam), FN1 (AF5335, Affinity Biotech), MMP2 (CSB-PA003258, Cusabio), MMP3 (17873-1-AP, Proteintech), MMP13 (CSB-PA07029A0Rb, Cusabio), ADAMTS-4 (DF6986, Affinity Biotech), ADAMTS-5 (DF13268, Affinity Biotech), p-p38 (AF4001, Affinity Biotech), p38 (14064-1-AP, Proteintech), p-JNK (AF3318, Affinity Biotech), JNK (AF6319, Affinity Biotech), p-ERK1/2 (sc-81492, Santa Cruz, Dallas, DX, USA), ERK1/2 (16443-1-AP, Proteintech).

    Techniques: